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Merck
CN

236284

2-Nitroanisole

≥99%

Synonym(s):

1-Methoxy-2-nitrobenzene

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About This Item

Linear Formula:
O2NC6H4OCH3
CAS Number:
91-23-6
Molecular Weight:
153.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854160
EC Number:
202-052-1
Beilstein/REAXYS Number:
1868032
MDL number:
MFCD00007096

Key Documents

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Product Name

2-Nitroanisole, ≥99%

InChI key

CFBYEGUGFPZCNF-UHFFFAOYSA-N

InChI

1S/C7H7NO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3

SMILES string

COc1ccccc1[N+]([O-])=O

assay

≥99%

form

liquid

refractive index

n20/D 1.561 (lit.)

bp

273 °C (lit.)

mp

9-12 °C (lit.)

solubility

alcohol: soluble(lit.)
diethyl ether: soluble(lit.)
water: insoluble(lit.)

density

1.254 g/mL at 25 °C (lit.)

functional group

nitro

Quality Level

100

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Application

2-Nitroanisole has been employed as solvatochromic probe to examine cybotactic region of pure and mixed supercritical fluid solvent systems.

General description

2-Nitroanisole (2-methoxynitrobenzene is an industrial and environmental pollutant causing tumors of the urinary bladder in rats and mice. Tumorigenic potential of 2-nitroanisole has been evaluated by host-mediated in vitro and in vivo assay.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

hcodes

H302,H350

Hazard Classifications

Acute Tox. 4 Oral - Carc. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKBX3796V
MKBZ4523V
MKBW1983V
MKBW1982V
MKBV8168V

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T Prabhu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 8-16 (2011-10-04)
Fourier-transform Raman and infrared spectra of 2-nitroanisole are recorded (4000-100 cm(-1)) and interpreted by comparison with respective theoretical spectra calculated using HF and DFT method. The geometrical parameters with C(S) symmetry, harmonic vibrational frequencies, infrared and Raman scattering intensities are
A Esmaeili et al.
Anticancer research, 26(6B), 4203-4212 (2007-01-05)
The host-mediated in vitro/in vivo assay system was used to evaluate the tumorigenic potential of the aromatic nitro compound 2-nitroanisole (2-NA). After intraperitoneal administration of the compound, resident macrophages were recovered by peritoneal lavage from treated and untreated mice and
Characterization of supercritical fluid solvents using solvatochromic shifts.
Yonker CR, et al.
The Journal of Physical Chemistry, 90(13), 3022-3026 (1986)
Mohammad Asaduzzaman Miah et al.
Ecology and evolution, 7(14), 5032-5040 (2017-08-05)
Cytochrome P450 monooxygenases (CYPs) usually overexpressed in resistant strain were found involved in oxidative detoxification of insecticides. In this study, an investigation was conducted to confirm if resistance irrelevant CYPs which were not overexpressed in resistant strain before, were capable
R D Irwin et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 30(1), 1-12 (1996-03-01)
o-Nitroanisole, a mutagenic intermediate used in the manufacture of azo dyes, was administered in feed for 2 years at concentrations of 0, 222, 666, or 2000 ppm to groups of 60 male and 60 female F344 rats. No significant increase
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